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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

D-Valine, N-[(4-methylphenyl)sulfonyl]-

CC([C@H](C(=O)O)NS(=O)(=O)c1ccc(cc1)C)C Request for Quotation
Chemical Name: D-Valine, N-[(4-methylphenyl)sulfonyl]-
CAS Number: 68005-71-0
Product Number: AG00FDWB(AGN-PC-0OGF6I)
Synonyms:
MDL No:
Molecular Formula: C12H17NO4S
Molecular Weight: 271.33268

Identification/Properties

Computed Properties
Molecular Weight:
271.331g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
5
Exact Mass:
271.088g/mol
Monoisotopic Mass:
271.088g/mol
Topological Polar Surface Area:
91.8A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
377
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Tos-D-Val-OH is a versatile reagent commonly used in chemical synthesis for the protection of amino groups in peptide chemistry. By utilizing Tos-D-Val-OH, chemists are able to selectively mask amino functionalities, allowing for the controlled manipulation of peptide structures during synthesis. This reagent is particularly valuable in the production of complex peptides and pharmaceuticals, where precise control over chemical reactions is crucial for the yield and quality of the final product. Furthermore, Tos-D-Val-OH offers excellent stability and compatibility with a wide range of reaction conditions, making it a valuable tool for synthetic chemists seeking efficient and reliable methods for peptide synthesis.